Product image of Humulin N (Insulin Human (Rdna)) supplied by GNH India

Humulin N

Active Ingredient:
Insulin Human (Rdna)
Origin:
EU

Humulin N (Insulin Human (Rdna))

Humulin N is a recombinant DNA insulin human product supplied as a 100 IU/mL injectable suspension for subcutaneous administration. It is a prescription‑only antidiabetic agent marketed in the European Union and belongs to the insulin drug class, used to replace or supplement endogenous insulin in diabetes management.

Manufacturer / TM Owner

Eli Lilly Hrvatska D.O.O.

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Indications & Clinical Uses

Humulin N is indicated for the long‑acting control of blood glucose in patients with diabetes. It is commonly employed in the following clinical situations:

  • Basal insulin therapy for type 1 diabetes mellitus.
  • Basal insulin therapy for type 2 diabetes mellitus.
  • Combination with rapid‑acting insulin analogues for intensive insulin regimens.
  • Use in adults, adolescents, and children when a stable, prolonged insulin effect is required.
  • Adjunct to diet and exercise for overall glycaemic management.

How It Works

  • Humulin N provides exogenous human insulin that binds to insulin receptors on cell membranes, activating the intrinsic tyrosine kinase activity. This triggers downstream signaling pathways, including the PI3K‑Akt cascade, which promotes translocation of GLUT‑4 transporters to the cell surface, enhances glucose uptake in muscle and adipose tissue, and suppresses hepatic gluconeogenesis, thereby lowering plasma glucose concentrations.

Side Effects

Adverse reactions to Humulin N vary in frequency and severity.

Common

  • Injection site redness, swelling, or bruising.
  • Low blood glucose (hypoglycaemia) episodes.
  • Weight gain.
  • Lipodystrophy at injection sites.

Serious

  • Severe hypoglycaemia with neuroglycopenic symptoms.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Persistent hypoglycaemia unresponsive to carbohydrate intake.
  • Edema or heart failure exacerbation in susceptible patients.

Precautions & Warnings

When prescribing or using Humulin N, consider the following precautions:

  • Assess renal and hepatic function, as impairment may alter insulin requirements.
  • Monitor for signs of hypoglycaemia, especially in patients with irregular meals or increased physical activity.
  • Use caution in pregnant or breastfeeding individuals; safety data are limited.
  • Adjust doses when initiating or discontinuing concomitant medications that affect glucose metabolism.
  • Educate patients on proper injection technique to reduce lipodystrophy risk.
  • Review cardiovascular status, as fluid retention may worsen heart failure.

Avoid Interactions

Humulin N may interact with several drug classes.

Avoid

  • Concurrent use of other insulin products without dose adjustment, which can precipitate severe hypoglycaemia.
  • Beta‑blockers that mask hypoglycaemia symptoms.

Use with caution

  • Oral hypoglycaemic agents (e.g., sulfonylureas, meglitinides) that increase insulin secretion.
  • Corticosteroids, which raise blood glucose and may require higher insulin doses.
  • Diuretics, particularly thiazides, that can impair glucose tolerance.
  • ACE inhibitors or ARBs, which may potentiate insulin’s glucose‑lowering effect.
  • Alcohol, which can cause unpredictable glucose fluctuations.

Frequently Asked Questions

Humulin N is a recombinant human insulin formulated as a long‑acting injectable suspension, providing basal insulin coverage.

It is injected subcutaneously, typically into the abdomen, thigh, or upper arm, using a suitable needle or pen device.

Patients with type 1 or type 2 diabetes who need a stable, long‑acting insulin to maintain basal glucose control may be prescribed Humulin N.

Safety data are limited; clinicians should weigh potential benefits against risks and monitor glucose closely if used in pregnancy.

Common signs include sweating, shakiness, confusion, irritability, rapid heartbeat, and in severe cases, loss of consciousness or seizures.

Rotate injection sites within the same region (e.g., abdomen) and avoid re‑using the exact spot to reduce lipodystrophy.

Yes, drugs such as sulfonylureas or meglitinides can increase the risk of hypoglycaemia and may require dose adjustments.

Store unopened vials in a refrigerator (2‑8 °C). Once in use, keep at room temperature, away from direct heat and light, and discard after the labeled period.

No, Humulin N is not classified as a controlled substance; it is a prescription‑only medication.

If a dose is missed, administer it as soon as remembered unless it is near the time of the next scheduled dose; do not double the dose.

Alcohol can cause unpredictable blood glucose changes and may increase the risk of hypoglycaemia when combined with insulin.

Insulin promotes glucose storage and can increase appetite, leading to weight gain in some patients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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